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(E)-1-(4-Hydroxy-benzo[b]thiophen-5-yl)-3-(4-methoxy-phenyl)-propenone

中文名称
——
中文别名
——
英文名称
(E)-1-(4-Hydroxy-benzo[b]thiophen-5-yl)-3-(4-methoxy-phenyl)-propenone
英文别名
(E)-1-(4-hydroxybenzothiophen-5-yl)-3-(4-methoxyphenyl)prop-2-en-1-one;(E)-1-(4-hydroxy-1-benzothiophen-5-yl)-3-(4-methoxyphenyl)prop-2-en-1-one
(E)-1-(4-Hydroxy-benzo[b]thiophen-5-yl)-3-(4-methoxy-phenyl)-propenone化学式
CAS
——
化学式
C18H14O3S
mdl
——
分子量
310.373
InChiKey
BNVAZNJFYLVSSB-XBXARRHUSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    4.9
  • 重原子数:
    22
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    74.8
  • 氢给体数:
    1
  • 氢受体数:
    4

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    (E)-1-(4-Hydroxy-benzo[b]thiophen-5-yl)-3-(4-methoxy-phenyl)-propenone氢氧化钾双氧水 作用下, 以 乙醇 为溶剂, 以65%的产率得到3-Hydroxy-2-(4-methoxy-phenyl)-thieno[2,3-h]chromen-4-one
    参考文献:
    名称:
    Synthesis of 4-hydroxy-1-methylindole and benzo[b]thiophen-4-ol based unnatural flavonoids as new class of antimicrobial agents☆
    摘要:
    Synthesis of nitrogen and sulfur heterocyclic mimics of furanoflavonoids have been achieved for the first time. Synthesized flavonoid alkaloids and thiophenyl flavonoids have been screened for antifungal and antibacterial activities. All the test compounds barring 25 exhibited antifungal activity. The compound 19 was the best and showed comparable MICs to the known compound karanjin. Compounds 5, 12, 14 and 22 also showed comparable MIC to karanjin. (C) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2004.12.032
  • 作为产物:
    描述:
    1-(4-羟基-1-苯并噻吩-5-基)乙酮4-甲氧基苯甲醛barium dihydroxide 作用下, 以 乙醇 为溶剂, 反应 3.0h, 以65%的产率得到(E)-1-(4-Hydroxy-benzo[b]thiophen-5-yl)-3-(4-methoxy-phenyl)-propenone
    参考文献:
    名称:
    Synthesis of 4-hydroxy-1-methylindole and benzo[b]thiophen-4-ol based unnatural flavonoids as new class of antimicrobial agents☆
    摘要:
    Synthesis of nitrogen and sulfur heterocyclic mimics of furanoflavonoids have been achieved for the first time. Synthesized flavonoid alkaloids and thiophenyl flavonoids have been screened for antifungal and antibacterial activities. All the test compounds barring 25 exhibited antifungal activity. The compound 19 was the best and showed comparable MICs to the known compound karanjin. Compounds 5, 12, 14 and 22 also showed comparable MIC to karanjin. (C) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2004.12.032
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文献信息

  • Synthesis of 4-hydroxy-1-methylindole and benzo[b]thiophen-4-ol based unnatural flavonoids as new class of antimicrobial agents☆
    作者:Prem P. Yadav、Prasoon Gupta、A.K. Chaturvedi、P.K. Shukla、Rakesh Maurya
    DOI:10.1016/j.bmc.2004.12.032
    日期:2005.3.1
    Synthesis of nitrogen and sulfur heterocyclic mimics of furanoflavonoids have been achieved for the first time. Synthesized flavonoid alkaloids and thiophenyl flavonoids have been screened for antifungal and antibacterial activities. All the test compounds barring 25 exhibited antifungal activity. The compound 19 was the best and showed comparable MICs to the known compound karanjin. Compounds 5, 12, 14 and 22 also showed comparable MIC to karanjin. (C) 2005 Elsevier Ltd. All rights reserved.
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